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Training memory without aversion: Appetitive hole-board spatial learning increases adult hippocampal neurogenesis
Patricia Sampedro-Piquero1, Román D Moreno-Fernández1, M Carmen Mañas-Padilla2
1Departamento de Psicobiología y Metodología de las Ciencias del Comportamiento, Instituto de Investigación Biomédica de Málaga (IBIMA), Facultad de Psicología, Universidad de Málaga, Spain.
Appetitive spatial learning in mice reduced cell proliferation but increased immature neurons, enhancing adult hippocampal neurogenesis (AHN). This appetitive learning potentiates AHN and hippocampal plasticity, minimizing stress.
Area of Science:
- Neuroscience
- Behavioral Neuroscience
- Neuroplasticity
Background:
- Adult hippocampal neurogenesis (AHN) is modulated by learning experiences.
- Most studies use aversive tasks (e.g., water maze), introducing stress as a confounder.
- The effects of appetitive learning on AHN remain largely unknown.
Purpose of the Study:
- To investigate how appetitive spatial learning in a hole-board maze affects AHN (cell proliferation, immature neurons).
- To examine the impact on hippocampal neuroplasticity markers (BDNF, IGF-II, CREB phosphorylation).
- To establish a paradigm for studying AHN and plasticity while minimizing aversive variables.
Main Methods:
- Mice were trained in a food-rewarded hole-board maze (Trained), exposed to a non-learning version (Pseudotrained), or a no-reward control (Control).
- Assessed spatial reference and working memory performance.
- Quantified AHN using immunohistochemistry and hippocampal protein expression via western blot.
Main Results:
- Trained mice showed reduced cell proliferation but increased immature neurons compared to controls.
- Enhanced AHN in Trained mice correlated with spatial reference memory performance.
- Trained animals exhibited increased hippocampal expression of BDNF, IGF-II, and phosphorylated CREB.
Conclusions:
- Appetitive spatial learning in the hole-board maze shifts AHN from proliferation to enhanced survival of young neurons.
- This task is a valuable model for studying AHN and hippocampal plasticity, mitigating stress-related confounds.
- The findings highlight the potential of appetitive learning to modulate neurogenesis and plasticity.
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